Vitamin D3 for the Treatment of Low Vitamin D in Cystic Fibrosis
Primary Purpose
Cystic Fibrosis, Vitamin D Deficiency
Status
Withdrawn
Phase
Phase 3
Locations
Study Type
Interventional
Intervention
cholecalciferol
Sponsored by
About this trial
This is an interventional treatment trial for Cystic Fibrosis focused on measuring cystic fibrosis, vitamin d, inflammation
Eligibility Criteria
Inclusion Criteria:
- Subjects age 10-25 years
- cystic fibrosis
- 25-(OH)-D < 20 ng/mL
- FEV1 > 40% -
Exclusion Criteria:
- inability to perform pulmonary function or hand-grip tests
- liver disease (including cirrhosis and portal hypertension) or baseline liver enzymes 21/2-fold greater than the upper limit of normal
- acute use of glucocorticoids at time of testing
- acute pulmonary exacerbation at time of testing
- known non-adherence to enzyme replacement
- hypercalcemia
- engages in "suntanning
Sites / Locations
Outcomes
Primary Outcome Measures
serum 25-hydroxy vitamin D levels
Secondary Outcome Measures
body composition
inflammatory markers
muscles strength
Full Information
NCT ID
NCT00762918
First Posted
September 26, 2008
Last Updated
February 19, 2010
Sponsor
Children's Hospital of Philadelphia
1. Study Identification
Unique Protocol Identification Number
NCT00762918
Brief Title
Vitamin D3 for the Treatment of Low Vitamin D in Cystic Fibrosis
Official Title
Vitamin D and Its Non-Classic Roles in Cystic Fibrosis
Study Type
Interventional
2. Study Status
Record Verification Date
February 2010
Overall Recruitment Status
Withdrawn
Why Stopped
Recruitment
Study Start Date
March 2008 (undefined)
Primary Completion Date
September 2008 (Actual)
Study Completion Date
September 2008 (Anticipated)
3. Sponsor/Collaborators
Name of the Sponsor
Children's Hospital of Philadelphia
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Vitamin D deficiency is common in cystic fibrosis. Vitamin D deficiency frequently persists despite aggressive treatment with ergocalciferol, a vitamin D preparation also known as vitamin D2. Cholecalciferol, a vitamin D preparation also known as vitamin D3,may work better to increase vitamin D levels.
Vitamin D is important for absorption of calcium from the diet and bone health. Vitamin D more recently has been found to play a role in regulating the normal inflammatory process. Since cystic fibrosis is a state of excessive inflammation, vitamin D may be playing a role in cystic fibrosis.
We hypothesize: cholecalciferol will work better to increase vitamin D levels in patients iwth cystic fibrosis and that it will have an effect on markers of inflammation.
Detailed Description
Vitamin D deficiency is common in cystic fibrosis (CF) and persists despite relatively high doses of ergocalciferol, vitamin D2. Replacement has traditionally been focused upon maintenance of calcium and phosphorus homeostasis and bone health. However, non-classic roles of vitamin D have become increasingly recognized and the contribution of vitamin D deficiency to non-bone disorders has become apparent. Vitamin D deficiency has been associated with increased risk of a variety of cancers, autoimmune diseases such as Type 1 diabetes and multiple sclerosis, Type 2 diabetes, tuberculosis, and myopathy. The connection between vitamin D and these disease states likely reflects vitamin D's role as a transcriptional regulator: it participates in cell cycle regulation and in the innate immune system mediates cathelicidin production following activation of toll-like receptors.One hallmark of CF is pulmonary hyper-inflammation with recurrent infections. Additionally, malnutrition and decreased lean muscle mass threaten pulmonary function in CF. While vitamin D and its relation to bone has been explored in CF, the role of vitamin D in inflammation, lean body mass and strength, and pulmonary muscle strength has not been investigated. Moreover, vitamin D replacement has traditionally been with ergocalciferol, vitamin D2. Vitamin D3, cholecalciferol, has a longer half-life and is considered more potent. Thus, cholecalciferol treatment of children and young adults with CF and vitamin D deficiency may be useful for attaining normal vitamin D status and for exploring the impact of vitamin D upon lean body mass, pulmonary muscle strength, and inflammation.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cystic Fibrosis, Vitamin D Deficiency
Keywords
cystic fibrosis, vitamin d, inflammation
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
0 (Actual)
8. Arms, Groups, and Interventions
Intervention Type
Dietary Supplement
Intervention Name(s)
cholecalciferol
Other Intervention Name(s)
Vitamin D3
Intervention Description
cholecalciferol 5000 IU capsule by mouth daily for 3 months
Primary Outcome Measure Information:
Title
serum 25-hydroxy vitamin D levels
Time Frame
3 months
Secondary Outcome Measure Information:
Title
body composition
Time Frame
3 months
Title
inflammatory markers
Time Frame
3 months
Title
muscles strength
Time Frame
3 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
10 Years
Maximum Age & Unit of Time
25 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Subjects age 10-25 years
cystic fibrosis
25-(OH)-D < 20 ng/mL
FEV1 > 40% -
Exclusion Criteria:
inability to perform pulmonary function or hand-grip tests
liver disease (including cirrhosis and portal hypertension) or baseline liver enzymes 21/2-fold greater than the upper limit of normal
acute use of glucocorticoids at time of testing
acute pulmonary exacerbation at time of testing
known non-adherence to enzyme replacement
hypercalcemia
engages in "suntanning
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Andrea Kelly, MD
Organizational Affiliation
Children's Hospital of Philadelphia
Official's Role
Principal Investigator
12. IPD Sharing Statement
Learn more about this trial
Vitamin D3 for the Treatment of Low Vitamin D in Cystic Fibrosis
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